All individuals with variants in gene CACNA1D

32 entries on 1 page. Showing entries 1 - 32.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 2 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 3 1 Yu Sun
00064726 - - - F - Denmark - 27y - - - SUD - 1 1 Sofie Lindgren Christiansen
00100458 - - - M no Germany white - - - - autism - 1 1 Joerg Striessnig
00100607 21131953-FamDEM9 PubMed: Baig 2011, Journal: Baig 2011 4-generation family, 4 affecteds (F, 3M), unaffected heterozygous carrier parents F;M yes Pakistan - - - - - SANDD see paper; ..., congenital deafness, bradycardia 1 4 Johan den Dunnen
00100608 21131953-FamDEM81 PubMed: Baig 2011, Journal: Baig 2011 6-generation family, 3 affecteds (3M), unaffected heterozygous carrier parents/sibs M yes Pakistan - - - - - SANDD see paper; ..., congenital deafness, bradycardia 1 3 Johan den Dunnen
00100609 21131953-con PubMed: Baig 2011, Journal: Baig 2011 255 healthy control subjects F;M - Pakistan - - - - - Healthy/Control - 1 1 Johan den Dunnen
00100610 23913001-FamK1444Pat1 PubMed: Scholl 2013, Journal: Scholl 2013 2-generation family, 1 affected, unaffected non-carrier parents F no United States European - - - - PASNA 0d-hypertension, biventricular hypertrophy, ventricular septal defect, pulmonary hypertension, second-degree heart block; elevated aldosterone levels, high aldosterone/renin ratio; uncontrolled hypertension, hypokalemia; treatment with calcium channel blocker, amlodipine, normalized blood pressure, and biventricular hypertrophy resolved; seizure disorder, apparent cerebral palsy, cortical blindness, complex neuromuscular abnormalities 1 1 Johan den Dunnen
00100611 23913001-FamK1555Pat1 PubMed: Scholl 2013, Journal: Scholl 2013 2-generation family, 1 affected, unaffected non-carrier parents/sibs F - United States African American - - - - PASNA 0d-cerebral palsy, spastic quadriplegia, mild athetosis, severe generalized intellectual disability, complex partial and generalized seizures; 5y-markedly hypertensive, persistently elevated blood pressure, polydipsia, hypokalemia, metabolic alkalosis, high serum aldosterone; CT-scan no adrenal abnormality; ECG mild left ventricular hypertrophy 1 1 Johan den Dunnen
00100612 23913001-APA37 PubMed: Scholl 2013, Journal: Scholl 2013 - - - United States - - - - - APA adrenal aldosterone-producing adenomas (APAs) 1 1 Johan den Dunnen
00100613 23913001-APA29 PubMed: Scholl 2013, Journal: Scholl 2013 - - - United States - - - - - APA adrenal aldosterone-producing adenomas (APAs) 1 1 Johan den Dunnen
00100614 23913001-APA31 PubMed: Scholl 2013, Journal: Scholl 2013 - - - United States - - - - - APA adrenal aldosterone-producing adenomas (APAs) 1 1 Johan den Dunnen
00100615 23913001-APA65 PubMed: Scholl 2013, Journal: Scholl 2013 - - - United States - - - - - APA adrenal aldosterone-producing adenomas (APAs) 1 1 Johan den Dunnen
00100616 23913001-APA59 PubMed: Scholl 2013, Journal: Scholl 2013 - - - United States - - - - - APA adrenal aldosterone-producing adenomas (APAs) 1 1 Johan den Dunnen
00180187 29286531-Pat39 PubMed: Tumienė 2018 - - - (Slovenia) - - - - - ? Epilepsy (HP:0001250), generalized tonic-clonic seizures (HP:0025190), left ventricular hypertrophy (HP:0001712), horseshoe kidney (HP:0000085), facial dysmorphism (HP:0001999), neuroblastoma (HP:0003006). 1 1 Johan den Dunnen
00282312 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282313 - PubMed: Scholl 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00282314 - PubMed: Baig 2011 - - - - - - - - - deafness brachycardia 1 1 Global Variome, with Curator vacancy
00282315 - PubMed: Iossifov 2012 - - - - - - - - - autism - 1 1 Global Variome, with Curator vacancy
00282316 - PubMed: O'Roak 2012, PubMed: Pinggera 2015, PubMed: Uddin 2014 - - - - - - - - - autism - 1 1 Global Variome, with Curator vacancy
00282317 - PubMed: Scholl 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00282318 - PubMed: Febbo 2011, PubMed: Hampel 2015, PubMed: Sturgeon 2008, PubMed: Carter 2013, PubMed: Evaluation of Genomic Applications in Practice and Prevention (EGAPP Working Group. 2014, PubMed: Lindberg 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00293447 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 15 Mohammed Faruq
00293448 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00293449 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 173 Mohammed Faruq
00293450 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 123 Mohammed Faruq
00304957 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304958 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00362025 PME_FI_G12 PubMed: Courage 2021, Journal: Courage 2021 - - - - - - - - - epilepsy - 1 1 Johan den Dunnen
00407694 ? PubMed: Fahim 2012 Ninety-eight affected males from 56 families - - - - - - - - retinal disease - 1 1 LOVD
00412172 patient Török et al., 2022, submitted - - - United States - - - - - PASNA 4 week old male infant: no seizures, but severe jittering at birth, episodes of hypoglycemia, pulmonary hypertension and arterial hypertension, elevated plasma aldosterone 1 1 Joerg Striessnig
00431535 251533 - - F no Germany - - - - - PASNA Hyperkalemia, Pseudohypoaldosteronism, Hypertension 1 1 Andreas Laner
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